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Data / Medical devices / Transport Systems, Anaerobic

Transport Systems, Anaerobic (JTX): 4 FDA-registered makers in 2 countries

4 establishments in 2 countries are registered with the FDA to make Transport Systems, Anaerobic (product code JTX, Class 1, 21 CFR 866.2900). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 8 510(k) clearances under this code, the latest on July 16, 1990, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
JTX
Device class
1
Regulation
866.2900
Medical specialty
Microbiology

Makers by country

CountryMakers
United States3
Italy1

Makers of Transport Systems, Anaerobic

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Arx SciencesAmherst, NY, United StatesManufacturer0000api.fda.gov
Copan ItaliaBRESCIA Lombardy, ItalyManufacturer0000api.fda.gov
Copan Industries, Inc.Aguadilla, PR, United StatesContract manufacturer0000api.fda.gov
Puritan Medical Products Company LLCGuilford, ME, United StatesContract manufacturer, Manufacturer0000api.fda.gov

Updated July 16, 1990. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.